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achromatopsia [2025/11/12 15:21] – created Scott Larsonachromatopsia [2025/12/01 17:17] (current) – [Resources] Scott Larson
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 ====== Achromatopsia ====== ====== Achromatopsia ======
  
 +====Main Features====
 +  * Reduced vision due to lack of functioning cones
 +    * Vision usually 20/200 with complete color blindness in complete forms 
 +    * Incomplete forms may have better vision and some color vision
 +  * Nystagmus that may improve with age
 +  * Central relative scotoma with normal peripheral visual fields
 +  * Complete and Incomplete forms
 +  * Usually stable but some see slow worsening of visual acuity and macular atrophy
 +====Distinguishing Features====
 +  * Photophobia at birth or early infancy 
 +  * Better vision in dim illumination
 +  * Sluggish pupil responses with paradoxical constriction in the dark 
 +  * Usually normal fundus appearance 
 +    * OCT may show ellipsoid zone disruption or absence, outer retinal atrophy and RPE loss
 +  * ERG 
 +    * lack of cone function- 30 Hz flicker and single flash photoptic waveform is small and delayed 
 +    * normal ROD function- normal dark adapted dim and bright flash waveforms
 +====Differential Dx====
 +  * [[congenital_stationary_night_blindness|Congenital Stationary Night Blindness]]
 +  * [[leber_congenital_amaurosis|Leber Congenital Amaurosis]]
 +  * [[retinitis_pigmentosa|Retinitis Pigmentosa]]
 +  * Idiopathic Nystagmus Syndrome 
 +====Pathogenesis====
 +  * 1 in 30,000 live births
 +  * Recessively inherited mutation in a gene that codes for a part of the cone phototransduction pathway. 
 +  * 70-80% from mutations in the following genes: CNGA3 and CNGB3 
 +  * 1-2% from mutations in GNAT2, PDE6C, PDE6H, ATF6 
 +====Treatment====
 +  * Supportive care
 +  * Sunglasses
 +====Resources====
 +  - [[https://www.clinicalkey.com/#!/content/book/3-s2.0-B9780702082986000457#hl0000659|Taylor and Hoyt Textbook article]]
 +  - [[https://www.tandfonline.com/doi/full/10.1080/13816810.2017.1418389 |Hirji N. et al. Achromatopsia: clinical features, molecular genetics, animal models and theraputic options. Ophthalmic Genetics 2018;39(2):149-157]] [[https://1drv.ms/b/c/31d83ae8e55e0542/EdksFbEMfIBMkILEHEs01NcB3l10U7_oZE0oUhaTNeVNVA?e=aWa9GE|_]]
  
 {{tag>inherited_retinal_disease retina}} {{tag>inherited_retinal_disease retina}}